Qualified Person (QP) – Full Time (w/m/d)

About the role

Acino AG, based in Munich, is part of the Acino Group, a Swiss pharmaceutical company and a leader in advanced drug delivery technologies. The role is to certify and release batches of medicinal products ensuring compliance with GMP and regulatory requirements.

Key responsibilities

• Certify each batch of medical product in accordance with Marketing Authorization, GMP and applicable regulations.
• Oversee batch release activities and ensure proper investigation and documentation of deviations and CAPAs.
• Maintain oversight of the supply chain to prevent distribution of non‑compliant or falsified medicines.
• Ensure third‑party manufacturers and suppliers comply with GMP standards.
• Perform batch certification and release in line with ethical and legal standards.
• Contribute as a member of a quality‑focused team.

Required profile

• University degree in Pharmacy, Chemistry or related life sciences.
• Recognized Qualified Person status with valid authorization from health authorities.
• Proven experience in the pharmaceutical industry and pharmacovigilance (GVP).
• Fluent in German and English with excellent written and verbal communication.
• Strong understanding of regulatory requirements and quality standards.

Required skills

• Digital Quality Management System (QMS) proficiency.
• Laboratory Information Management System (LIMS) familiarity.
• Good Pharmacovigilance Practice (GVP) knowledge.

What we offer

• International working environment in a growing company.
• Motivated, agile and service‑oriented team.
• Diverse tasks providing a broad basis for future career development.
• Attractive salary.
• Flexible working hours with the possibility of home office.